Unique transcriptomic response to sepsis is observed among patients of different age groups

• Published in: PloS one 2017-09, Vol.12 (9), p.e0184159-e0184159
• Main Authors: Raymond, Steven L, López, María Cecilia, Baker, Henry V, Larson, Shawn D, Efron, Philip A, Sweeney, Timothy E, Khatri, Purvesh, Moldawer, Lyle L, Wynn, James L
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Adults; Age; Age Factors; Age groups; Aged; Bacterial infections; Biology and Life Sciences; Case-Control Studies; Child; Child, Preschool; Children; Computational Biology - methods; Critical care; Datasets; Diagnostic systems; Female; Gene expression; Gene Expression Profiling; Gene Expression Regulation; Genome-Wide Association Study; Genomes; Human behavior; Humans; Immunology; Incidence; Infant; Infant, Newborn; Infants; Inflammation; Informatics; Male; Medicine; Medicine and Health Sciences; Middle Aged; Morbidity; Mortality; Neonates; Neutrophils; Newborn babies; Patients; Pediatrics; People and Places; Physiology; Sepsis; Sepsis - genetics; Sepsis - microbiology; Statistical analysis; Studies; Surgery; Transcriptome; Young Adult
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0184159

Sepsis is a major cause of morbidity and mortality, especially at the extremes of age. To understand the human age-specific transcriptomic response to sepsis, a multi-cohort, pooled analysis was conducted on adults, children, infants, and neonates with and without sepsis. Nine public whole-blood gene expression datasets (636 patients) were employed. Age impacted the transcriptomic host response to sepsis. Gene expression from septic neonates and adults was more dissimilar whereas infants and children were more similar. Neonates showed reductions in inflammatory recognition and signaling pathways compared to all other age groups. Likewise, adults demonstrated decreased pathogen sensing, inflammation, and myeloid cell function, as compared to children. This may help to explain the increased incidence of sepsis-related organ failure and death in adults. The number of dysregulated genes in septic patients was proportional to age and significantly differed among septic adults, children, infants, and neonates. Overall, children manifested a greater transcriptomic intensity to sepsis as compared to the other age groups. The transcriptomic magnitude for adults and neonates was dramatically reduced as compared to children and infants. These findings suggest that the transcriptomic response to sepsis is age-dependent, and diagnostic and therapeutic efforts to identify and treat sepsis will have to consider age as an important variable.